RESUMO
Normal leaf margin development is important for leaf morphogenesis and contributes to diverse leaf shapes in higher plants. We here show the crucial roles of an atypical type II phosphatidylinositol 4-kinase, PI4Kγ5, in Arabidopsis leaf margin development. PI4Kγ5 presents a dynamics expression pattern along with leaf development and a T-DNA mutant lacking PI4Kγ5, pi4kγ5-1, presents serrated leaves, which is resulted from the accelerated cell division and increased auxin concentration at serration tips. Studies revealed that PI4Kγ5 interacts with and phosphorylates a membrane-bound NAC transcription factor, ANAC078. Previous studies demonstrated that membrane-bound transcription factors regulate gene transcription by undergoing proteolytic process to translocate into nucleus, and ANAC078 undergoes proteolysis by cleaving off the transmembrane region and carboxyl terminal. Western blot analysis indeed showed that ANAC078 deleting of carboxyl terminal is significantly reduced in pi4kγ5-1, indicating that PI4Kγ5 is important for the cleavage of ANAC078. This is consistent with the subcellular localization observation showing that fluorescence by GFP-ANAC078 is detected at plasma membrane but not nucleus in pi4kγ5-1 mutant and that expression of ANAC078 deleting of carboxyl terminal, driven by PI4Kγ5 promoter, could rescue the leaf serration defects of pi4kγ5-1. Further analysis showed that ANAC078 suppresses the auxin synthesis by directly binding and regulating the expression of auxin synthesis-related genes. These results indicate that PI4Kγ5 interacts with ANAC078 to negatively regulate auxin synthesis and hence influences cell proliferation and leaf development, providing informative clues for the regulation of in situ auxin synthesis and cell division, as well as the cleavage and functional mechanism of membrane-bound transcription factors.
Assuntos
1-Fosfatidilinositol 4-Quinase/genética , Proteínas de Arabidopsis/genética , Ácidos Indolacéticos/metabolismo , Desenvolvimento Vegetal/genética , Fatores de Transcrição/genética , 1-Fosfatidilinositol 4-Quinase/biossíntese , Arabidopsis/genética , Arabidopsis/crescimento & desenvolvimento , Proteínas de Arabidopsis/biossíntese , Divisão Celular/genética , Proliferação de Células/genética , DNA Bacteriano/genética , Regulação da Expressão Gênica de Plantas , Mutação , Folhas de Planta/genética , Folhas de Planta/crescimento & desenvolvimento , Plantas Geneticamente Modificadas , Fatores de Transcrição/biossínteseRESUMO
Yeast phosphatidylinositol-transfer protein (Sec14p) is essential for Golgi secretory function and cell viability. This requirement of Sec14p is relieved by genetic inactivation of the cytidine diphosphate-choline pathway for phosphatidycholine (PtdCho) biosynthesis. Standard phenotypic analyses indicate that inactivation of the phosphatidylethanolamine (PtdEtn) pathway for PtdCho biosynthesis, however, does not rescue the growth and secretory defects associated with Sec14p deficiency. We now report inhibition of choline uptake from the media reveals an efficient "bypass Sec14p" phenotype associated with PtdEtn-methylation pathway defects. We further show that the bypass Sec14p phenotype associated with PtdEtn-methylation pathway defects resembles other bypass Sec14p mutations in its dependence on phospholipase D activity. Finally, we find that increased dosage of enzymes that catalyze phospholipase D-independent turnover of PtdCho, via mechanisms that do not result in a direct production of phosphatidic acid or diacylglycerol, effect a partial rescue of sec14-1(ts)-associated growth defects. Taken together, these data support the idea that PtdCho is intrinsically toxic to yeast Golgi secretory function.
Assuntos
Proteínas de Transporte/metabolismo , Proteínas Fúngicas/metabolismo , Complexo de Golgi/metabolismo , Proteínas de Membrana , Proteínas de Membrana Transportadoras , Fosfatidilcolinas/metabolismo , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/crescimento & desenvolvimento , 1-Fosfatidilinositol 4-Quinase/biossíntese , 1-Fosfatidilinositol 4-Quinase/genética , Transporte Biológico , Proteínas de Transporte/genética , Colina/metabolismo , Meios de Cultura , Proteínas Fúngicas/biossíntese , Proteínas Fúngicas/genética , Expressão Gênica , Lisofosfolipase , Metilação , Fosfatidiletanolaminas/metabolismo , Proteínas de Transferência de Fosfolipídeos , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismoRESUMO
Phosphatidylinositol (PI) and its phosphorylated derivatives, collectively called phosphoinositides, are important second messengers involved in a variety of cellular processes, including cell proliferation, apoptosis, metabolism, and migration. These derivatives are generated by a family of kinases called phosphoinositide lipid kinases (PIKs). Due to the central role of these kinases in signaling pathways, assays for measuring their activity are often used for drug development. Lipid kinase substrates are present in unique membrane environments in vivo and are insoluble in aqueous solutions. Therefore the most important consideration in developing successful lipid kinase assays is the physical state of lipid kinase substrates. Here we describe the preparation of lipid substrates for two major classes of lipid kinases, phosphatidylinositol 3-kinases (PI3Ks) and phosphatidylinositol 4-kinases (PI4Ks). Using PI4Ks as an example, we also provide a detailed protocol for small-scale kinase expression and affinity purification from transiently transfected mammalian cells. For measuring lipid kinase activity we apply a universal bioluminescent ADP detection approach. The approach is compatible with diverse lipid substrates and can be used as a single integrated platform for measuring all classes of lipid and protein kinases.
Assuntos
1-Fosfatidilinositol 4-Quinase/análise , Difosfato de Adenosina/análise , Medições Luminescentes/métodos , Fosfatidilinositol 3-Quinases/análise , Fitas Reagentes , 1-Fosfatidilinositol 4-Quinase/biossíntese , 1-Fosfatidilinositol 4-Quinase/genética , 1-Fosfatidilinositol 4-Quinase/isolamento & purificação , Células HEK293 , Humanos , Indicadores e Reagentes , Luciferases de Vaga-Lume/metabolismo , Micelas , Fosfatidilinositol 3-Quinases/biossíntese , Fosfatidilinositol 3-Quinases/genética , Fosfatidilinositol 3-Quinases/isolamento & purificação , Fosfatidilinositóis/metabolismo , Proteínas Recombinantes de Fusão/biossíntese , Proteínas Recombinantes de Fusão/isolamento & purificação , Especificidade por Substrato , TransfecçãoRESUMO
By constructing DNA probes we have identified and cloned a human PtdIns 4-kinase, PI4K230, corresponding to a mRNA of 7.0 kb. The cDNA encodes a protein of 2044 amino acids. The C-terminal part of ca. 260 amino acids represents the catalytic domain which is highly conserved in all recently cloned PtdIns 4-kinases. N-terminal motifs indicate multiple heterologous protein interactions. Human PtdIns 4-kinase PI4K230 expressed in vitro exhibits a specific activity of 58 micromol mg-1min-1. The enzyme expressed in Sf9 cells is essentially not inhibited by adenosine, it shows a high Km for ATP of about 300 microM and it is half-maximally inactivated by approximately 200 nM wortmannin. These data classify this enzyme as type 3 PtdIns 4-kinase. Antibodies raised against the N-terminal part moderately activate and those raised against the C-terminal catalytic domain inhibit the enzymatic activity. The coexistence of two different type 3 PtdIns 4-kinases, PI4K92 and PI4K230, in several human tissues, including brain, suggests that these enzymes are involved in distinct basic cellular functions.
Assuntos
1-Fosfatidilinositol 4-Quinase/genética , 1-Fosfatidilinositol 4-Quinase/biossíntese , 1-Fosfatidilinositol 4-Quinase/química , Sequência de Aminoácidos , Sequência de Bases , Northern Blotting , Linhagem Celular , Clonagem Molecular , Humanos , Isoenzimas/biossíntese , Isoenzimas/química , Isoenzimas/genética , Dados de Sequência MolecularRESUMO
Our studies of renal phosphoinositide levels and metabolism in the pcy mouse with polycystic kidney disease (PKD) suggest that phosphatidylinositol kinase (PtdInsK) and phospholipase C (PLC) are elevated in this renal disorder. Therefore, the steady-state levels of select isoforms of these enzymes were examined in renal cytosolic and particulate (detergent-soluble) fractions in male and female normal and CD1-pcy/pcy (pcy) mice at 60, 120 and 180 days of age, and in male and female normal and diseased (Han:SPRD-cy) rats at 28 and 70 days of age. Disease-related increases in phosphatidylinositol 4-kinasebeta (PtdIns4Kbeta) and PLC(gamma1) levels were present in both models. PtdIns4Kbeta levels were higher by as much as 233% in pcy mice and by 95% in diseased Han:SPRD-cy rats compared to normals of the same age and gender. Steady-state levels of PLC(gamma1) were as much as 74% and 35% higher in pcy mice and diseased Han:SPRD-cy rats, respectively, compared to their controls. The consistency of these alterations in two accepted models of PKD indicates the importance of the phosphoinositide signalling pathway in the evolution of this disorder, and represents a potential site for therapeutic intervention.
Assuntos
1-Fosfatidilinositol 4-Quinase/biossíntese , Rim/metabolismo , Doenças Renais Policísticas/metabolismo , 1-Fosfatidilinositol 4-Quinase/análise , Fatores Etários , Animais , Modelos Animais de Doenças , Feminino , Isoenzimas/análise , Isoenzimas/biossíntese , Rim/enzimologia , Rim/patologia , Fígado/enzimologia , Fígado/metabolismo , Masculino , Camundongos , Tamanho do Órgão , Fosfatidilinositol 3-Quinases/análise , Fosfatidilinositol 3-Quinases/biossíntese , Fosfolipase C gama , Doenças Renais Policísticas/enzimologia , Doenças Renais Policísticas/patologia , Ratos , Frações Subcelulares/metabolismo , Fosfolipases Tipo C/análise , Fosfolipases Tipo C/biossínteseRESUMO
Transient forebrain ischemia induces a delayed neuronal death in the CA1 area of the hippocampus. However, the mechanism leading to this phenomenon has yet to be established. The authors used an mRNA differential-display method to isolate genes for which mRNA levels change only in the hippocampus during ischemia/reperfusion. They succeeded in identifying the product of one down-regulated gene as phosphatidylinositol 4-kinase (PI 4-K). Compared with control levels, PI 4-K mRNA expression in the hippocampus, but not the cerebral cortex, was significantly decreased by 30% and about 80% 1 and 7 days after ischemia/reperfusion, respectively. Interestingly, PI 4-K and PI bisphosphate levels were selectively decreased in the CA1 region, but not other regions, whereas TUNEL-positive cells could be detected 3 days after ischemia. Consistent with these results, PI 4-K expression was suppressed by hypoxia in SK-N-MC neuroblastoma cells before loss of cell viability. Overexpression of wild-type PI 4-K, but not the kinase-negative mutant of PI 4-K (K1789A), recovered the loss of viability induced by hypoxia. These findings strongly suggest that a prior decrease in PI 4-K and PI bisphosphate levels caused by brain ischemia/hypoxia is partly involved in delayed neuronal cell death.
Assuntos
1-Fosfatidilinositol 4-Quinase/biossíntese , Isquemia Encefálica/fisiopatologia , Morte Celular/fisiologia , Hipocampo/fisiologia , Neurônios/fisiologia , Prosencéfalo/irrigação sanguínea , Animais , Northern Blotting , Córtex Cerebral/fisiologia , DNA Complementar/análise , Imuno-Histoquímica , Masculino , Ratos , Ratos WistarRESUMO
BACKGROUND: Studies have shown that periodontal ligament fibroblasts (PDLF) and gingival fibroblasts (GF) respond differently to growth factors in the repair and regeneration of periodontal tissues. The goal of this study was to determine the effects of insulin-like growth factor-1 (IGF-1) signaling on cell apoptosis in PDLF compared to GF. METHODS: The levels of apoptosis were compared between cultured PDLF and GF by DNA fragmentation assay and trypan blue exclusion assay, either in the presence or absence of IGF-1. The transcript level of upstream signaling molecules, such as IGF binding protein-5 (IGFBP-5), IGF-1 receptor (IGF-1R), and phosphoinositide 3-kinase (PI3K), was studied using reverse transcription-polymerase chain reaction (RT-PCR). Furthermore, the role of IGFBP-5 in IGF-1 signaling was verified by annexin-V staining using flow cytometric analysis. RESULTS: IGF-1 significantly inhibited the level of DNA fragmentation and decreased trypan blue-positive cells in PDLF compared to GF during serum deprivation. The mRNA expression of IGFBP-5, IGF-1R, and PI3K was constitutively upregulated in PDLF compared to GF. In the presence of exogenous IGFBP-5, the annexin-V-positive cells were significantly decreased in GF after IGF-1 stimulation. CONCLUSIONS: The present study provides evidence that IGF-1 reduces apoptosis in cultured PDLF compared to GF. Upregulation of IGF-1R and PI3K in PDLF further suggests the activation of IGF signaling in PDLF. In addition, the anti-apoptotic effect of IGF-1 may be facilitated by the upregulation of IGFBP-5 in PDLF.
Assuntos
Apoptose/fisiologia , Gengiva/citologia , Fator de Crescimento Insulin-Like I/fisiologia , Ligamento Periodontal/citologia , 1-Fosfatidilinositol 4-Quinase/biossíntese , Apoptose/efeitos dos fármacos , Células Cultivadas , Fibroblastos/citologia , Humanos , Proteína 5 de Ligação a Fator de Crescimento Semelhante à Insulina/biossíntese , Proteína 5 de Ligação a Fator de Crescimento Semelhante à Insulina/farmacologia , Proteína 5 de Ligação a Fator de Crescimento Semelhante à Insulina/fisiologia , Fator de Crescimento Insulin-Like I/farmacologia , RNA Mensageiro/biossíntese , Receptor IGF Tipo 1/biossíntese , Proteínas Recombinantes/farmacologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transdução de Sinais , Regulação para CimaRESUMO
Endemic nephropathy has been linked to exposure of ochratoxin-A (OA) in grains and animal products. The underlying events surrounding this form of renal injury are not well known, partly due to the lack of a suitable animal model of the disease. Therefore, in this study, a pig model of OA-induced renal injury was established and used to examine whether elements of the phosphoinositide signalling pathway are altered in this disease. Weanling piglets were fed diets containing 0, 2, and 4 ppm OA for 6 weeks. Serum creatinine and urea and renal fibrosis were monitored biweekly using serial blood samples and renal biopsies. At termination, the protein levels of renal phosphatidylinositol 4-kinase-beta (PtdIns4Kbeta) and phospholipase C(gamma1) (PLC(gamma1)) were determined using immunoblotting and scanning densitometry. Serum creatinine was elevated by 2 weeks and renal fibrosis was elevated by 4 weeks at both levels of inclusion of OA. At the end of the experimental period, kidney size and water content were elevated, as were the protein levels of renal PtdIns4Kbeta and PLC(gamma1) in OA-exposed animals. Therefore, serial biopsies can be used to track changes in renal pathology in the OA-exposed piglet. We conclude that this is a useful model for OA-induced renal injury in which the underlying molecular events associated with this form of renal injury can be studied.
Assuntos
1-Fosfatidilinositol 4-Quinase/biossíntese , Fibrose/induzido quimicamente , Rim/patologia , Ocratoxinas/farmacologia , Fosfolipases Tipo C/biossíntese , 1-Fosfatidilinositol 4-Quinase/imunologia , Animais , Dieta , Modelos Animais de Doenças , Indução Enzimática/efeitos dos fármacos , Feminino , Fibrose/enzimologia , Formaldeído , Immunoblotting/métodos , Rim/efeitos dos fármacos , Rim/enzimologia , Fígado/efeitos dos fármacos , Fígado/enzimologia , Fígado/patologia , Masculino , Inclusão em Parafina , Fosfolipase C gama , Transdução de Sinais/efeitos dos fármacos , Suínos , Extratos de Tecidos/química , Fixação de Tecidos , Fosfolipases Tipo C/imunologiaRESUMO
Membrane lipids have been implicated in many critical cellular processes, yet little is known about the role of asymmetric lipid distribution in cell morphogenesis. The phosphoinositide bis-phosphate PI(4,5)P(2) is essential for polarized growth in a range of organisms. Although an asymmetric distribution of this phospholipid has been observed in some cells, long-range gradients of PI(4,5)P(2) have not been observed. Here, we show that in the human pathogenic fungus Candida albicans a steep, long-range gradient of PI(4,5)P(2) occurs concomitant with emergence of the hyphal filament. Both sufficient PI(4)P synthesis and the actin cytoskeleton are necessary for this steep PI(4,5)P(2) gradient. In contrast, neither microtubules nor asymmetrically localized mRNAs are critical. Our results indicate that a gradient of PI(4,5)P(2), crucial for filamentous growth, is generated and maintained by the filament tip-localized PI(4)P-5-kinase Mss4 and clearing of this lipid at the back of the cell. Furthermore, we propose that slow membrane diffusion of PI(4,5)P(2) contributes to the maintenance of such a gradient.
Assuntos
Citoesqueleto de Actina/fisiologia , Candida albicans/crescimento & desenvolvimento , Candida albicans/patogenicidade , Hifas/crescimento & desenvolvimento , Fosfatidilinositol 4,5-Difosfato/biossíntese , 1-Fosfatidilinositol 4-Quinase/biossíntese , 1-Fosfatidilinositol 4-Quinase/genética , Citoesqueleto de Actina/enzimologia , Candida albicans/genética , Polaridade Celular/fisiologia , Proteínas Fúngicas/biossíntese , Proteínas Fúngicas/genética , Hifas/enzimologia , Fosfatidilinositol 4,5-Difosfato/metabolismo , Fosfotransferases (Aceptor do Grupo Álcool)/biossíntese , Fosfotransferases (Aceptor do Grupo Álcool)/genéticaRESUMO
The oncoprotein c-Fos is a well-recognized AP-1 transcription factor. In addition, this protein associates with the endoplasmic reticulum and activates the synthesis of phospholipids. However, the mechanism by which c-Fos stimulates the synthesis of phospholipids in general and the specific lipid pathways activated are unknown. Here we show that induction of quiescent cells to reenter growth promotes an increase in the labeling of polyphosphoinositides that depends on the expression of c-Fos. We also investigated whether stimulation by c-Fos of the synthesis of phosphatidylinositol and its phosphorylated derivatives depends on the activation of enzymes of the phosphatidylinositolphosphate biosynthetic pathway. We found that c-Fos activates CDP-diacylglycerol synthase and phosphatidylinositol (PtdIns) 4-kinase II α in vitro, whereas no activation of phosphatidylinositol synthase or of PtdIns 4-kinase II ß was observed. Both coimmunoprecipitation and fluorescence resonance energy transfer experiments consistently showed a physical interaction between the N-terminal domain of c-Fos and the enzymes it activates.
Assuntos
Fosfatos de Fosfatidilinositol/biossíntese , Proteínas Proto-Oncogênicas c-fos/metabolismo , Fator de Transcrição AP-1/metabolismo , 1-Fosfatidilinositol 4-Quinase/biossíntese , 1-Fosfatidilinositol 4-Quinase/genética , Animais , Diacilglicerol Colinofosfotransferase/biossíntese , Diacilglicerol Colinofosfotransferase/genética , Ativação Enzimática/fisiologia , Indução Enzimática/fisiologia , Camundongos , Células NIH 3T3 , Fosfatos de Fosfatidilinositol/genética , Fosfolipídeos/biossíntese , Fosfolipídeos/genética , Estrutura Terciária de Proteína/fisiologia , Proteínas Proto-Oncogênicas c-fos/genética , Fator de Transcrição AP-1/genéticaRESUMO
Successful completion of cytokinesis relies on addition of new membrane, and requires the recycling endosome regulator Rab11, which localizes to the midzone. Despite the critical role of Rab11 in this process, little is known about the formation and composition of Rab11-containing organelles. Here, we identify the phosphatidylinositol (PI) 4-kinase III beta four wheel drive (Fwd) as a key regulator of Rab11 during cytokinesis in Drosophila melanogaster spermatocytes. We show Fwd is required for synthesis of PI 4-phosphate (PI4P) on Golgi membranes and for formation of PI4P-containing secretory organelles that localize to the midzone. Fwd binds and colocalizes with Rab11 on Golgi membranes, and is required for localization of Rab11 in dividing cells. A kinase-dead version of Fwd also binds Rab11 and partially restores cytokinesis to fwd mutant flies. Moreover, activated Rab11 partially suppresses loss of fwd. Our data suggest Fwd plays catalytic and noncatalytic roles in regulating Rab11 during cytokinesis.
Assuntos
1-Fosfatidilinositol 4-Quinase/metabolismo , Citocinese , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/enzimologia , Espermatócitos/enzimologia , Proteínas rab de Ligação ao GTP/metabolismo , 1-Fosfatidilinositol 4-Quinase/biossíntese , 1-Fosfatidilinositol 4-Quinase/genética , Animais , Células COS , Chlorocebus aethiops , Drosophila melanogaster/genética , Fertilidade , Complexo de Golgi/enzimologia , Isoenzimas , Masculino , Microscopia de Fluorescência , Ligação Proteica , Proteínas Recombinantes de Fusão/metabolismo , Vesículas Secretórias/enzimologia , Transfecção , Técnicas do Sistema de Duplo-Híbrido , Proteínas rab de Ligação ao GTP/genéticaRESUMO
Human phosphatidylinositol 4-kinase, isoform PI4K92, was expressed as His6 tagged protein in Sf9 cells reaching a level of approximately 5% of cellular protein. The enzyme can be purified nearly to homogeneity in a single step by absorption/desorption on Ni/nitriloacetic acid agarose magnetic beads. High Km values in the millimolar range for ATP and PtdIns as well as only a moderate inhibition by adenosine and a sensitivity to Wortmannin (IC50 approximately 300 nM) characterize the enzyme as a type 3 PI4K. The enzyme produces PtdIns4P as product. The isolated enzyme is a phosphoprotein, additionally phosphate is incorporated by incubation with ATP/Mg or ATP/Mn. Phosphorylation sites were mapped by MALDI-MS and LC-MS/MS at the following positions: S258, T263, S266, S277, S294, T423, S496, T504. Accordingly, a stretch of 81 amino acids between the common and the C-terminal catalytic domain was designated phosphorylation domain.